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A case report of recurrent Well’s syndrome masquerading as cellulitis

Eosinophilic cellulitis (Well’s syndrome) is a rare relapsing inflammatory disorder characterized by infiltration of eosinophils into the dermis. Although rare, WS should be considered in patients with a history of asthma and skin lesions that are resistant to antibiotic therapy. We report a case of...

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Autores principales: Qureshi, Anum, Manley, Jasmine, Flack, Tristan, Lowitt, Mark H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604493/
https://www.ncbi.nlm.nih.gov/pubmed/34804409
http://dx.doi.org/10.1080/20009666.2021.1979737
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author Qureshi, Anum
Manley, Jasmine
Flack, Tristan
Lowitt, Mark H.
author_facet Qureshi, Anum
Manley, Jasmine
Flack, Tristan
Lowitt, Mark H.
author_sort Qureshi, Anum
collection PubMed
description Eosinophilic cellulitis (Well’s syndrome) is a rare relapsing inflammatory disorder characterized by infiltration of eosinophils into the dermis. Although rare, WS should be considered in patients with a history of asthma and skin lesions that are resistant to antibiotic therapy. We report a case of recurrent WS. A 67-year-old woman with a history of asthma presented with a longstanding left pretibial ulcer with surrounding erythema, pain, and serous drainage, which had failed treatment with oral and parenteral antibiotics. Skin biopsy revealed eosinophilic cellulitis. Rapid improvement occurred with systemic steroid treatment; however, recurrent disease in the perineum developed as corticosteroids were tapered.
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spelling pubmed-86044932021-11-20 A case report of recurrent Well’s syndrome masquerading as cellulitis Qureshi, Anum Manley, Jasmine Flack, Tristan Lowitt, Mark H. J Community Hosp Intern Med Perspect Case Report Eosinophilic cellulitis (Well’s syndrome) is a rare relapsing inflammatory disorder characterized by infiltration of eosinophils into the dermis. Although rare, WS should be considered in patients with a history of asthma and skin lesions that are resistant to antibiotic therapy. We report a case of recurrent WS. A 67-year-old woman with a history of asthma presented with a longstanding left pretibial ulcer with surrounding erythema, pain, and serous drainage, which had failed treatment with oral and parenteral antibiotics. Skin biopsy revealed eosinophilic cellulitis. Rapid improvement occurred with systemic steroid treatment; however, recurrent disease in the perineum developed as corticosteroids were tapered. Taylor & Francis 2021-11-15 /pmc/articles/PMC8604493/ /pubmed/34804409 http://dx.doi.org/10.1080/20009666.2021.1979737 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of Greater Baltimore Medical Center. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Qureshi, Anum
Manley, Jasmine
Flack, Tristan
Lowitt, Mark H.
A case report of recurrent Well’s syndrome masquerading as cellulitis
title A case report of recurrent Well’s syndrome masquerading as cellulitis
title_full A case report of recurrent Well’s syndrome masquerading as cellulitis
title_fullStr A case report of recurrent Well’s syndrome masquerading as cellulitis
title_full_unstemmed A case report of recurrent Well’s syndrome masquerading as cellulitis
title_short A case report of recurrent Well’s syndrome masquerading as cellulitis
title_sort case report of recurrent well’s syndrome masquerading as cellulitis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604493/
https://www.ncbi.nlm.nih.gov/pubmed/34804409
http://dx.doi.org/10.1080/20009666.2021.1979737
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